Product Recalls in Nebraska

Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,524 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,524 in last 12 months

Showing 1710117120 of 28,140 recalls

Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 80" (203 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 84" (213 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 137" (348 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 175" (445 cm) Y-Type Blood Set w/170 Micron Blood Filter Recalled by ICU...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 125" (318 cm) Bifuse Blood Set w/170 Micron Filter Recalled by ICU Medical,...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· Cook Inc.

Recalled Item: Central Venous Tray Triple Lumen Polyurethane Catheter Recalled by Cook Inc....

The Issue: Central venous catheters may not fit over guide wire potentially causing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 98" (249 cm) Y-Type Admin Set w/170 Micron Blood Filter Recalled by ICU...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 84" Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical, Inc. Due...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· Cook Inc.

Recalled Item: Central Venous Catheter Set Heparin Coated Triple Lumen Polyurethane...

The Issue: Central venous catheters may not fit over guide wire potentially causing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 128" (325 cm) Y-Type Blood Set with 170 Micron Filter Recalled by ICU...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 32" (81 cm) Appx 4.4 mL Recalled by ICU Medical, Inc. Due to Some devices...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 120" (305cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 100" (254 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· Cook Inc.

Recalled Item: Central Venous Catheter Set Triple Lumen Polyurethane Recalled by Cook Inc....

The Issue: Central venous catheters may not fit over guide wire potentially causing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· Cook Inc.

Recalled Item: Central Venous Catheter Tray Triple Lumen Polyurethane Recalled by Cook Inc....

The Issue: Central venous catheters may not fit over guide wire potentially causing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 119" Blood Set w/200 Micron Filter Recalled by ICU Medical, Inc. Due to Some...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 159" (404 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· Cook Inc.

Recalled Item: Spectrum Central Venous Catheter Tray Minocycline/Rifampin Antibiotic...

The Issue: Central venous catheters may not fit over guide wire potentially causing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 88" (224 cm) Y-Type Blood Set w/200 Micron Filter Recalled by ICU Medical,...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· Oakworks Inc

Recalled Item: Foot Controls impacted for the following devices: OAKWORKS¿ Medical CFPM...

The Issue: The foot control used on the OAKWORKS¿ Inc., CFPM300, CFPM301, CFPM400,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing